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jam5435-sup-0001-TableS1.docWord document41KTable S1 Combinations of L. monocytogenes strains and plasmid-borne promoter fusions investigated in this study.
jam5435-sup-0002-TableS2.docxWord document17KTable S2 Primers used for quantitative real-time PCR.
jam5435-sup-0003-TableS3.pdfapplication/PDF251KTable S3 Examples of the growth/no growth boundary in an agar assay with L. monocytogenes for all tested antibiotics shown both on white and black background showing up- or down-regulation, respectively.
jam5435-sup-0004-TableS4.docxWord document24KTable S4 The impact of the antibiotics measures as the diameter of the inhibition zones. Each strain was measure in the agar-based screening assay with a minimum of two replicates expect in BHI with activated charcoal, which was only performed once. The diameter of inhibition zone is including the antibiotic disc, which is 6 mm in diameter.
jam5435-sup-0005-TableS5.docxWord document616KTable S5 Listeria monocytogenes with empty control vectors pTCV-lac and pSOG30222 (no promoter fusions) in response to all 16 antibiotics. Bacterial cells were diluted 1000-fold prior to being cast in BHI agar.
jam5435-sup-0006-TableS6.docxWord document17KTable S6 The effect of different classes of antibiotics on the gene expression of selected virulence or stress genes in L. monocytogenes EGD wild-type or regulator mutant strains.

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